Accord 71340013Recalls & reported problems
Smith & Nephew, Inc. · ACCORD STANDARD 265MM 11 CABLE TROCHANTERIC GRIP · Class 2 · Implant
All models of Accord (14)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 03596010485823), received between May 3, 2017 and May 15, 2025 — classified as 3 injuries.
The most frequently reported specific device problem is “Break” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Break1
- Fracture1
Patient problems
- No Information2
- Discomfort1
- Nonunion/Delayed-union Bone Fracture1
- Pain1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryMay 15, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT AFTER THR SURGERY HAD BEEN PERFORMED ON (B)(6) 2024, THE PATIENT EXPERIENCED PAIN, DISCOMFORT, AND A FRACTURE ALONG WITH ONE (1) ACC STD 265MM 11 CBL TRCH GRIP. ACCORDING TO THE SURGEON, BONE UNION WAS ATTEMPTED WITH THE ACCORD GRIP, BUT THE FRACTURE DID NOT INTEGRATE. THIS ADVERSE EVENT WAS RESOLVED BY A REVISION SURGERY ON (B)(6) 2025, IN WHICH THE LINER AND INSERT WERE EXCHANGED TO OR3O DUAL MOBILITY LINER 38/50 AND OR3O DUAL MOBILITY XLPE INSERT 28/38 RESPECTIVELY, AND THE CUP WAS EXCHANGED TO R3 MULTI HOLE ACETABULAR SHELL 50MM. THE HEAD AND STEM WERE EXCHANGED TO COMPETITOR COMPONENTS. THE CURRENT HEALTH STATUS OF THE PATIENT REMAINS UNKNOWN.
Patient problems: Discomfort; Nonunion/Delayed-union Bone Fracture; Pain
MAUDE report 22025096 ↗InjuryDec 9, 2019Fracture; Fracture
IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED ON (B)(6) 2019 DUE TO IMPLANT BREAKAGE, A COMPETITOR STEM WAS BROKEN AS WELL.
Patient problems: No Information
MAUDE report 9440661 ↗InjuryMay 3, 2017Break; Break
IT WAS REPORTED A REVISION SURGERY WAS REQUIRED DUE TO HARDWARE FAILURE. THE FEMUR BUTTRESS PLATE BROKE.
Patient problems: No Information
MAUDE report 6541379 ↗
Other CERCLAGE, FIXATION devices
- ZipFix 03.501.080Synthes GmbH · CERCLAGE, FIXATION236 reports
- CONTROL 1739-28-000Depuy Orthopaedics, Inc. · CERCLAGE, FIXATION52 reports
- Dall-Miles 6704-0-110Howmedica Osteonics Corp. · CERCLAGE, FIXATION1 recall1 report
- Tritium® Sternal Cable Plate System 86-27-12-S12Pioneer Surgical Technology, Inc. · CERCLAGE, FIXATION1 recall0 reports
- Accord 71340007Smith & Nephew, Inc. · CERCLAGE, FIXATION47 reports
- ZipFix 08.501.001.01SSynthes GmbH · CERCLAGE, FIXATION39 reports
- NA 298.801.01SSynthes GmbH · CERCLAGE, FIXATION33 reports
- ZipFix 08.501.001.05SSynthes GmbH · CERCLAGE, FIXATION29 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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